Common genetic variation and the control of HIV-1 in humans.


Autoria(s): Fellay, J.; Ge, D.; Shianna, K.V.; Colombo, S.; Ledergerber, B.; Cirulli, E.T.; Urban, T.J.; Zhang, K.; Gumbs, C.E.; Smith, J.P.; Castagna, A.; Cozzi-Lepri, A.; De Luca, A.; Easterbrook, P.; Günthard, H.F.; Mallal, S.; Mussini, C.; Dalmau, J.; Martinez-Picado, J.; Miro, J.M.; Obel, N.; Wolinsky, S.M.; Martinson, J.J.; Detels, R.; Margolick, J.B.; Jacobson, L.P.; Descombes, P.; Antonarakis, S.E.; Beckmann, J.S.; O'Brien, S.J.; Letvin, N.L.; McMichael, A.J.; Haynes, B.F.; Carrington, M.; Feng, S.; Telenti, A.; Goldstein, D.B.
Data(s)

01/12/2009

Resumo

To extend the understanding of host genetic determinants of HIV-1 control, we performed a genome-wide association study in a cohort of 2,554 infected Caucasian subjects. The study was powered to detect common genetic variants explaining down to 1.3% of the variability in viral load at set point. We provide overwhelming confirmation of three associations previously reported in a genome-wide study and show further independent effects of both common and rare variants in the Major Histocompatibility Complex region (MHC). We also examined the polymorphisms reported in previous candidate gene studies and fail to support a role for any variant outside of the MHC or the chemokine receptor cluster on chromosome 3. In addition, we evaluated functional variants, copy-number polymorphisms, epistatic interactions, and biological pathways. This study thus represents a comprehensive assessment of common human genetic variation in HIV-1 control in Caucasians.

Identificador

https://serval.unil.ch/notice/serval:BIB_86D58F4F4348

info:pmid:20041166

https://serval.unil.ch/resource/serval:BIB_86D58F4F4348.P001/REF

http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_86D58F4F43489

urn:nbn:ch:serval-BIB_86D58F4F43489

http://my.unil.ch/serval/document/BIB_86D58F4F4348.pdf

http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_86D58F4F43489

Idioma(s)

eng

Direitos

info:eu-repo/semantics/openAccess

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Fonte

PLoS genetics512e1000791

Palavras-Chave #Adult; Alleles; Disease Progression; Female; Genetic Variation; Genotype; HIV Infections/virology; HIV-1/physiology; Humans; Kaplan-Meier Estimate; Major Histocompatibility Complex/genetics; Male; Phenotype; Polymorphism, Single Nucleotide/genetics; Viral Load
Tipo

info:eu-repo/semantics/article

article

Contribuinte(s)

NIAID Center for HIV/AIDS Vaccine Immunology (CHAVI)

Formato

application/pdf